[Effect of recombinant human erythropoietin on bcl-2 protein expression in the retina in a rabbit model of acute high intraocular pressure]

Nan Fang Yi Ke Da Xue Xue Bao. 2010 Mar;30(3):552-4.
[Article in Chinese]

Abstract

Objective: To investigate the effect of recombinant human erythropoietin (rhEPO) on the expression of bcl-2 protein in the retina of rabbits with acute high intraocular pressure and explore the mechanism underlying the protective effect of rhEPO on the retina against ischemia-reperfusion injury.

Methods: rhEPO was injected subcutaneously in the ear of a rabbit model of acute high intraocular pressure induced by physiological saline perfusion into the anterior chamber. Bcl-2 protein expression in the retina of the rabbits was observed by immunohistochemical staining on days 1, 3, 7, and 14 after retinal ischemia-reperfusion and compared with that in normal rabbits and untreated rabbit models.

Results: bcl-2-positive cells were observed in the retina of normal rabbits with a mean positive cell number of 10.5-/+1.2 in each high-power visual field. Compared with that in the normal control group, the number of the positive cells decreased significantly in both the model group and EPO group (P<0.05, P<0.01), but the latter group showed a significantly greater number than the former (P<0.05 at day 7 and P<0.01 at day 14).

Conclusion: Systemic administration of rhEPO can up-regulate the expression of bcl-2 protein in the retina of rabbits with acute high intraocular pressure, which is probably one of the mechanisms for the protective effect of rhEPO on the retina against ischemia-reperfusion injury.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Erythropoietin / pharmacology
  • Erythropoietin / therapeutic use*
  • Female
  • Humans
  • Male
  • Ocular Hypertension / drug therapy*
  • Ocular Hypertension / metabolism*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Rabbits
  • Random Allocation
  • Recombinant Proteins
  • Retina / metabolism*

Substances

  • Proto-Oncogene Proteins c-bcl-2
  • Recombinant Proteins
  • Erythropoietin